<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Evans JP</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>NICHD NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>1093-1102.e3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9035359</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(8)</volume><pubmed_abstract>Recent reports of SARS-CoV-2 Omicron variant sub-lineages, BA.1, BA.1.1, and BA.2, have reignited concern over potential escape from vaccine- and infection-induced immunity. We examine the sensitivity of these sub-lineages and other major variants to neutralizing antibodies from mRNA-vaccinated and boosted individuals, as well as recovered COVID-19 patients, including those infected with Omicron. We find that all Omicron sub-lineages, especially BA.1 and BA.1.1, exhibit substantial immune escape that is largely overcome by mRNA vaccine booster doses. While Omicron BA.1.1 escapes almost completely from neutralization by early-pandemic COVID-19 patient sera and to a lesser extent from sera of Delta-infected patients, BA.1.1 is sensitive to Omicron-infected patient sera. Critically, all Omicr</pubmed_abstract><journal>Cell host &amp; microbe</journal><pubmed_title>Neutralization of SARS-CoV-2 Omicron sub-lineages BA.1, BA.1.1, and BA.2.</pubmed_title><pmcid>PMC9035359</pmcid><funding_grant_id>R01 HD095881</funding_grant_id><funding_grant_id>UL1 TR002733</funding_grant_id><funding_grant_id>U54 CA260582</funding_grant_id><funding_grant_id>R01 HL096376</funding_grant_id><funding_grant_id>R01 AI150473</funding_grant_id><funding_grant_id>KL2 TR002734</funding_grant_id><pubmed_authors>Xu K</pubmed_authors><pubmed_authors>Faraone J</pubmed_authors><pubmed_authors>Evans JP</pubmed_authors><pubmed_authors>Mallampalli R</pubmed_authors><pubmed_authors>Gumina RJ</pubmed_authors><pubmed_authors>Zhou T</pubmed_authors><pubmed_authors>Mohler PJ</pubmed_authors><pubmed_authors>Zheng YM</pubmed_authors><pubmed_authors>Liu SL</pubmed_authors><pubmed_authors>Zeng C</pubmed_authors><pubmed_authors>Qu P</pubmed_authors><pubmed_authors>Saif LJ</pubmed_authors><pubmed_authors>Lozanski G</pubmed_authors><pubmed_authors>Carlin C</pubmed_authors><pubmed_authors>Oltz EM</pubmed_authors><pubmed_authors>Bednash JS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neutralization of SARS-CoV-2 Omicron sub-lineages BA.1, BA.1.1, and BA.2.</name><description>Recent reports of SARS-CoV-2 Omicron variant sub-lineages, BA.1, BA.1.1, and BA.2, have reignited concern over potential escape from vaccine- and infection-induced immunity. We examine the sensitivity of these sub-lineages and other major variants to neutralizing antibodies from mRNA-vaccinated and boosted individuals, as well as recovered COVID-19 patients, including those infected with Omicron. We find that all Omicron sub-lineages, especially BA.1 and BA.1.1, exhibit substantial immune escape that is largely overcome by mRNA vaccine booster doses. While Omicron BA.1.1 escapes almost completely from neutralization by early-pandemic COVID-19 patient sera and to a lesser extent from sera of Delta-infected patients, BA.1.1 is sensitive to Omicron-infected patient sera. Critically, all Omicr</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-05-31T21:00:19.235Z</modification><creation>2025-02-19T04:21:16.569Z</creation></dates><accession>S-EPMC9035359</accession><cross_references><pubmed>35526534</pubmed><doi>10.1016/j.chom.2022.04.014</doi></cross_references></HashMap>